ReadyProbes™ Reagent F-Actin Phalloidin Conjugates
ReadyProbes™ Reagent F-Actin Phalloidin Conjugates
Invitrogen™

ReadyProbes™ Reagent F-Actin Phalloidin Conjugates

Perfect for fixed cells and tissue, ReadyProbes Reagent F-actin phalloidin conjugates offer clear visualization of actin filaments, making it perfect for cell biology, neuroscience, cancer research, and more.
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Catalog NumberColorExcitation Wavelength Range
R37110Green495/518
R37112Red-Orange540/565
Catalog number R37110
Price (CLP)
331.684
Each
Add to cart
Color:
Green
Excitation Wavelength Range:
495/518
Price (CLP)
331.684
Each
Add to cart
ActinGreen 488 ReadyProbes Reagent is a selective, high-affinity F-actin probe conjugated to our bright, photostable, green-fluorescent Alexa Fluor 488 dye. ActinGreen 488 reagent is a room temperature-stable solution of Alexa Fluor 488 Phalloidin (Cat. No. A12379) packaged in a dropper bottle. ActinRed 555 ReadyProbes Reagent is a comparable F-actin stain conjugated to the red-orange fluorescent dye tetramethylrhodamine (TRITC). ActinRed 555 reagent is a room temperature-stable solution of Rhodamine Phalloidin (Cat. No. R415) packaged in a dropper bottle.

These ready-to-use solutions combines superior brightness with exceptional F-actin staining. Phalloidin is a bi-cyclic peptide, commonly used in imaging applications to selectively label F-actin. Fluorescently labeled phalloidin has several advantages over antibodies for actin labeling, including virtually identical binding properties with actin from different species of plants and animals and low non-specific binding.

Features

  • High-affinity staining of F-actin with superior specificity compared to antibody methods
  • ActinGreen 488 Excitation/Emission: (495/518 nm), detected through standard GFP and FITC filter sets
  • ActinRed 555 Excitation/Emission: (540/565 nm), detected through standard RFP and TRITC filters sets
  • Use counterstain (i.e., DAPI or NucBlue ReadyProbes reagent) as desired

ReadyProbes format advantages

  • Ready-to-use formulation—no need to dilute, weigh, or pipette
  • Just use two drops per mL of medium to stain, incubate 30 minutes, wash, then image
  • Stable at room temperature—keep handy on the benchtop

Applications

  • For fixed and permeabilized cells or tissue
  • Fluorescence microscopy (IF/IHC/ICC)
  • High content screening, high content imaging
  • Flow cytometry

Suggestions for use

  • Both ActinRed 555 and ActinGreen 488 reagents may be added directly to fixed cells in full medium or buffer solutions
  • In most cases 2 drops/mL and an incubation time of 15–30 minutes is sufficient for bright actin staining; however, optimization may be needed for some cell types, conditions, and applications. In such cases, simply add more or fewer drops until the optimal staining intensity is obtained.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
ColorGreen
DescriptionActinGreen™ 488 ReadyProbes™ Reagent (AlexaFluor™ 488 phalloidin)
Detection MethodFluorescence
Dye TypeAlexa Fluor™ 488
EmissionVisible
Excitation Wavelength Range495/518
For Use With (Equipment)Confocal Microscope, Floid™ Cell Imaging System, Fluorescence Microscope, Flow Cytometer, Floid™ Cell Imaging System
FormLiquid
Product LineActinGreen, ReadyProbes
Quantity1 kit
TechniqueFluorescence Intensity
Label TypeFluorescent Dye
Product TypePhalloidin
SubCellular LocalizationCytoskeleton
Unit SizeEach
Contents & Storage

2 x 2.5 mL dropper bottles

Store at ≤ 25°C.

Frequently asked questions (FAQs)

Can I use the ReadyProbes reagents for flow cytometry?

This is not recommended. The ReadyProbes reagents were developed for imaging applications whereas the Ready Flow reagents were optimized for flow cytometry.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Citations & References (40)

Citations & References
Abstract
Iridium oxide nanotube electrodes for sensitive and prolonged intracellular measurement of action potentials.
Authors:Lin ZC, Xie C, Osakada Y, Cui Y, Cui B,
Journal:
PubMed ID:24487777
'Intracellular recording of action potentials is important to understand electrically-excitable cells. Recently, vertical nanoelectrodes have been developed to achieve highly sensitive, minimally invasive and large-scale intracellular recording. It has been demonstrated that the vertical geometry is crucial for the enhanced signal detection. Here we develop nanoelectrodes of a new geometry, ... More
The cellular and proteomic response of primary and immortalized murine Kupffer cells following immune stimulation diverges from that of monocyte-derived macrophages.
Authors:Tweedell R, Tao D, Dinglasan RR,
Journal:
PubMed ID:25266554
Kupffer cells (KCs) are the first line of defense in the liver against pathogens, yet several microbes successfully target the liver, bypass immune surveillance, and effectively develop in this tissue. Our current, albeit poor, understanding of KC-pathogen interactions has been largely achieved through the study of primary cells, requiring isolation ... More
Distinct adipogenic differentiation phenotypes of human umbilical cord mesenchymal cells dependent on adipogenic conditions.
Authors:Saben J, Thakali KM, Lindsey FE, Zhong Y, Badger TM, Andres A, Shankar K,
Journal:
PubMed ID:24951473
The umbilical cord (UC) matrix is a source of multipotent mesenchymal stem cells (MSCs) that have adipogenic potential and thus can be a model to study adipogenesis. However, existing variability in adipocytic differentiation outcomes may be due to discrepancies in methods utilized for adipogenic differentiation. Additionally, functional characterization of UCMSCs ... More
CD8 T Cells Use IFN-? To Protect against the Lethal Effects of a Respiratory Poxvirus Infection.
Authors:Goulding J, Abboud G, Tahiliani V, Desai P, Hutchinson TE, Salek-Ardakani S,
Journal:
PubMed ID:24748494
CD8 T cells are a key component of immunity to many viral infections. They achieve this through using an array of effector mechanisms, but precisely which component/s are required for protection against a respiratory orthopox virus infection remains unclear. Using a model of respiratory vaccinia virus infection in mice, we ... More
An iron-regulated and glycosylation-dependent proteasomal degradation pathway for the plasma membrane metal transporter ZIP14.
Authors:Zhao N, Zhang AS, Worthen C, Knutson MD, Enns CA,
Journal:
PubMed ID:24927598
Protein degradation is instrumental in regulating cellular function. Plasma membrane proteins targeted for degradation are internalized and sorted to multivesicular bodies, which fuse with lysosomes, where they are degraded. ZIP14 is a newly identified iron transporter with multitransmembrane domains. In an attempt to dissect the molecular mechanisms by which iron ... More